Medical Device Manufacturer · US , Penngrove , CA

Microstim, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1991

Total

Cleared

Denied

Microstim, Inc. has 2 FDA 510(k) cleared medical devices. Based in Penngrove, US.

Historical record: 2 cleared submissions from 1991 to 2001. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Microstim, Inc. Filter by specialty or product code using the sidebar.

Microstim, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Microstim, Inc.

2 devices

1-2 of 2